GB1031407A - Improvements in or relating to polyesters - Google Patents
Improvements in or relating to polyestersInfo
- Publication number
- GB1031407A GB1031407A GB44423/64A GB4442364A GB1031407A GB 1031407 A GB1031407 A GB 1031407A GB 44423/64 A GB44423/64 A GB 44423/64A GB 4442364 A GB4442364 A GB 4442364A GB 1031407 A GB1031407 A GB 1031407A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acids
- acid
- polyester
- product
- bis
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/692—Polyesters containing atoms other than carbon, hydrogen and oxygen containing phosphorus
- C08G63/6924—Polyesters containing atoms other than carbon, hydrogen and oxygen containing phosphorus derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/6928—Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/68—Unsaturated polyesters
- C08G18/683—Unsaturated polyesters containing cyclic groups
- C08G18/686—Unsaturated polyesters containing cyclic groups containing cycloaliphatic groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/82—Preparation processes characterised by the catalyst used
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
A fire-retardant polyester resin is obtained by reacting dicyclopentadiene with the reaction product from (A) one or more dicarboxylic acids and/or ester-forming derivatives thereof, (B) one or more bromine-containing carboxylic acids, (C) one or more condensable phosphorus-containing compounds, and (D) one or more polyhydroxy compounds and/or ester-forming derivatives thereof, at least 20% of the total equivalents of acids and hydroxy compounds containing an olefinic bond, and the bromine and phosphorus together amounting to at least 2 weight per cent. The initial polyester preferably has an acid value of 70-150, falling after reaction with dicyclodiene to below 70, and to at least 20 less than the original value if this was 70-90. Preferably 0.05-0.6 mols. of dicyclopentadiene are used per mol. of dicarboxylic acid. The dicarboxylic acid (A) is preferably an a ,b -unsaturated dicarboxylic acid, e.g. maleic, fumaric, itaconic, mesaconic, or citraconic acids, or anhydrides or half-esters thereof with a polyhydric alcohol, but may contain preferably not more than 60 equivalent per cent of other acids, e.g. succinic, adipic, sebacic, azelaic, the phthalic and di-, tri-, and tetra-chloro phthalic acids, and tetrahydrophthalic acid, and chlorendic acid. Higher polybasic acids may be used in minor amounts, e.g. pyromellitic or trimellitic acid, the additional carboxy group(s) being esterified with monohydric alcohols. The poly-hydroxy compounds (D) may be, e.g. ethylene glycol, diethylene glycol, 1,2- or 1,3-propanediol, 2,2-dialkanepropadiols, 1,3- and 1,4 - butanediols, D 2.3 - butene - 1,4 - diol, 1,6 - hexanediol, dimethylolbenzenes, resorcinol, the 4,41 - dihydroxy - dicyclohexyl alkanes, the 4,41 - dihydroxy - diphenyl alkanes, trimethylolpropane, glycerol monochlorhydrin, pentaerythritol dichlorohydrin, pentachlorophenyl monoglycerol ether, 4,6-dibromo - resorcinol - bis - (b - hydroxyethyl) ether and 2,3 - bis - [dibromo - 4 - (b - hydroxyethoxy)phenyl] propane. Higher polyhydroxy alcohols may be used, e.g. glycerol, trimethylolpropane or -ethane, the additional hydroxy group(s) being etherified or esterified with monofunctional alcohols or acids. The bromine containing acids (B) are preferably polybasic with at least 2 Br atoms in the molecule, e.g. the bromine additions products of maleic, fumaric, itaconic, mesaconic, and citraconic acids, or of acrylic ricinoleic or linseed oil fatty acids, or di- and tetra-bromophthalic acids, hexabromoendomethylenetetrahydrophthalic acid, dibromohexahydrophthalic acid and dibromoendomethylenehexahydrophthalic acid. The phosphorus compounds (C) may be acids, thio acids, amides, organic oxides, sulphides, esters, thioesters and halides, and include phosphoric acid, phosphorous acid, pyrophosphoric acid, the phosphinic acids and the phosphonic acids and esters and halides thereof, and trimethylol phosphine oxide and tetramethylol phosphonium halides, phosphine sulphides, thiophosphites, thio- and dithio-phosphates, phosphonic amides, amido-phosphites and amido-phosphates. The product resins may be copolymerized with e.g. styrene, alkyland chloro-styrenes, a -methylstyrene, vinyl acetate or propionate, acrylic and methacrylic acid esters, allyl acetate or propionate, diallyl maleate, succinate, adipate, azelate, sebacate, or phthalate, triallyl phosphate, diallyl benzenphosphonate, triallyl cyanurate and N-vinylpyrrolidone. The ratio of vinyl compound to polyester may vary from 4:1 to 1:9, by weight. Conventional polymerization inhibitors, catalysts and accelerators may be used, or an accelerator such as aniline- or p-toluidine-N,N-diacetic acid or N,N-bis-(hydroxyethyl)-aniline or -p-toluidine may be incorporated into the polyester. The product polyesters may also be reacted with polyisocyanates, e.g. 4,41 - diphenylmethane -, 1,5 - naphthalene -, 2,21 - diphenyldimethylmethane - 4,41 -, toluylene-2,4 and toluylene-2,6-, and 1,4-cyclohexylene - diisocyanates, and 4,41,411 - triisocyanatophenyl thiophosphate. Fillers, e.g. asbestos, chalk, powdered glass, silicon carbide, sawdust, hardened plastics, calcium hydrogen phosphate, and glass, cotton, polyester or polyamide fibres, dyes and pigments may be incorporated into moulding compositions. In examples, maleic anhydride is condensed with phthalic anhydride (or bis-hydroxyethyl-terephthalate) and dibromosuccinic or dibromoitaconic acids or tetrabromophthalic anhydride or 9,10,12,13,15,16 - hexabromo - octadecanoic acid, and phosphoric acid or 2-hydroxypropane-2-phosphonic acid or a PCl3/ethylene glycol or vinyl phosphonic dichloride/2,2-dimethylpropanediol-1,3 reaction product, and glycerol, trimethylol propane or 2,2-dimethylpropanediol-1,3 in the presence of hydroquinone and triphenyl phosphite, and the product is reacted with dicyclopentadiene. This product in turn may be copolymerized with styrene (70:30 ratio).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEC0031270 | 1963-10-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1031407A true GB1031407A (en) | 1966-06-02 |
Family
ID=7019750
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB44423/64A Expired GB1031407A (en) | 1963-10-30 | 1964-10-30 | Improvements in or relating to polyesters |
Country Status (8)
Country | Link |
---|---|
US (1) | US3333022A (en) |
AT (1) | AT271013B (en) |
BE (1) | BE654876A (en) |
CH (1) | CH496753A (en) |
DE (1) | DE1495330A1 (en) |
GB (1) | GB1031407A (en) |
NL (1) | NL6412649A (en) |
SE (1) | SE324896B (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3619228A (en) * | 1966-07-25 | 1971-11-09 | Mac Millan Bloedel Ltd | Method of patching wood products using a particular polyester blend |
US3536782A (en) * | 1967-01-25 | 1970-10-27 | Diamond Shamrock Corp | Halogenated polyester compositions and process for preparing the same |
US3883612A (en) * | 1971-06-07 | 1975-05-13 | Scm Corp | Low-shrink thermosetting polymers |
US3933757A (en) * | 1973-02-08 | 1976-01-20 | Scm Corporation | Dicyclopentadiene thermosetting polyester |
US3992480A (en) * | 1973-07-30 | 1976-11-16 | Hooker Chemicals & Plastics Corporation | Fire retardant unsaturated polyesters |
JPS5640220A (en) * | 1979-09-10 | 1981-04-16 | Hitachi Chem Co Ltd | Manufacturing of flyback transformer |
US4525427A (en) * | 1982-09-20 | 1985-06-25 | The Alpha Corporation | Polyester primer composition and method |
US5043374A (en) * | 1988-03-25 | 1991-08-27 | Atochem North America, Inc. | Halogenated polyester flame retardants for polyphenylene ether, polyolefin and polyethylene terephthalate resins |
CN102227480B (en) | 2008-11-26 | 2014-09-03 | 威士伯采购公司 | Polyester-carbamate polymer and coating compositions thereof |
EP2370490B1 (en) | 2008-11-26 | 2018-07-18 | Valspar Sourcing, Inc. | Coating compositions comprising a polyester polymer |
US20100260954A1 (en) * | 2008-11-26 | 2010-10-14 | Valspar Sourcing, Inc. | Polymer having polycyclic groups and coating compositions thereof |
US8367171B2 (en) | 2008-11-26 | 2013-02-05 | Valspar Sourcing, Inc. | Polymer having polycyclic groups and coating compositions thereof |
ES2595990T3 (en) | 2009-04-09 | 2017-01-04 | Valspar Sourcing, Inc. | Polymer having unsaturated cycloaliphatic functionality and coating compositions formed therefrom |
CN102388080B (en) | 2009-04-09 | 2014-09-24 | 威士伯采购公司 | Polyester coating composition |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL274611A (en) * | 1951-01-28 | |||
US2671070A (en) * | 1951-12-08 | 1954-03-02 | Us Rubber Co | Reaction products of dicyclopentadiene, maleic anhydride, and a glycol, and copolymers thereof |
US2819247A (en) * | 1953-06-10 | 1958-01-07 | American Cyanamid Co | Flame-resistant polyester resinous compositions containing combined halogens and phosporus and process of preparation |
DE1178211B (en) * | 1955-01-29 | 1964-09-17 | C F Roser G M B H | Process for the production of unsaturated polyester |
US2852487A (en) * | 1955-08-05 | 1958-09-16 | Glidden Co | Polymerizable solution of an allyl ether and an unsaturated alkyd resin |
US2951823A (en) * | 1956-02-11 | 1960-09-06 | Ruetgerswerke Ag | Unsaturated polyesters of unsaturated alpha, beta-dicarboxylic acids and polyvalent alcohols |
DE1150203B (en) * | 1959-08-25 | 1963-06-12 | Distillers Co Yeast Ltd | Process for the production of an unsaturated polyester |
FR1317444A (en) * | 1962-02-12 | 1963-02-08 | Albert Ag Chem Werke | Process for preparing polyester resins |
-
1963
- 1963-10-30 DE DE19631495330 patent/DE1495330A1/en active Pending
-
1964
- 1964-10-19 US US404643A patent/US3333022A/en not_active Expired - Lifetime
- 1964-10-20 AT AT891264A patent/AT271013B/en active
- 1964-10-22 CH CH1367164A patent/CH496753A/en not_active IP Right Cessation
- 1964-10-23 SE SE12791/64A patent/SE324896B/xx unknown
- 1964-10-27 BE BE654876D patent/BE654876A/xx unknown
- 1964-10-30 GB GB44423/64A patent/GB1031407A/en not_active Expired
- 1964-10-30 NL NL6412649A patent/NL6412649A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
NL6412649A (en) | 1965-05-03 |
CH496753A (en) | 1970-09-30 |
BE654876A (en) | 1965-04-27 |
US3333022A (en) | 1967-07-25 |
DE1495330A1 (en) | 1969-02-27 |
SE324896B (en) | 1970-06-15 |
AT271013B (en) | 1969-05-27 |
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